LPL, lipoprotein lipase, 4023

N. diseases: 290; N. variants: 116
Disease: Apolipoprotein C-II Deficiency (disorder) ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1720779
Disease: Apolipoprotein C-II Deficiency (disorder)
Apolipoprotein C-II Deficiency (disorder) 		0.320 Biomarker disease BEFREE Familial chylomicronemia syndrome is a rare disorder of lipoprotein metabolism due to familial lipoprotein lipase (LPL) or apolipoprotein C-II deficiency or the presence of inhibitors to lipoprotein lipase. 17542893 2007
CUI: C1720779
Disease: Apolipoprotein C-II Deficiency (disorder)
Apolipoprotein C-II Deficiency (disorder) 		0.320 Biomarker disease BEFREE In most of these disorders, pancreatitis is not very common and, with the exception of lipoprotein lipase and apolipoprotein C-II deficiency, is neither the leading nor the clinically most distressing manifestation of the underlying metabolic defect. 12120223 2001
CUI: C1720779
Disease: Apolipoprotein C-II Deficiency (disorder)
Apolipoprotein C-II Deficiency (disorder) 		0.320 Biomarker disease CTD_human